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DELTA SCANNER, DELTA SCANNER PRO, DS SPINE PRO, DS SPORTS PRO AND DS REHAB

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071878
510(k) Type
Traditional
Applicant
MED-LECTRIC CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2007
Days to Decision
154 days
Submission Type
Summary

DELTA SCANNER, DELTA SCANNER PRO, DS SPINE PRO, DS SPORTS PRO AND DS REHAB

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071878
510(k) Type
Traditional
Applicant
MED-LECTRIC CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2007
Days to Decision
154 days
Submission Type
Summary